KMC Systems is looking for talented team players like you to help us turn our customers’ concepts and inventions into innovative, groundbreaking instrumentation.
KMC Systems has been recognized as one of the best companies to work for in New Hampshire by Business NH Magazine. We offer an employee-empowered culture with competitive benefits and career advancement, plus the opportunity to be a part of some of the healthcare industry’s most exciting breakthroughs. Check out the opportunities below and apply online today.
KMC Systems, Inc., is a wholly owned subsidiary of Elbit Systems of America. Elbit Systems of America, is proud to be an Equal Opportunity Employer.
Direct the KMC Quality System on a cross functional, interdepartmental basis and act as the primary interface with the US FDA regarding compliance, inspections and audits. Represent KMC in all discussions with current and potential customers regarding quality and regulatory issues, ensuring that performance and quality of products conform to established industry standards necessary to maintain lasting customer satisfaction. Ensures the highest quality standards and level of regulatory compliance with efficient, cost-effective and timely operations.View Details
Responsible for managing and allocating resources required to manufacture multi‑technology, high quality analytical and medical instruments at cost levels competitive with other instrument companies and customer's in‑house manufacturing capabilities. Maintain effective liaison with customers and all interfacing departments to provide optimum operations. Responsible for overall program management of transition programs to assure the company's successful contract performance.View Details
Do you have experience managing/supporting a complex instrument manufacturing environment in low volume, high mix environments? Can you lead a team of 10-12 Manufacturing Engineers, proactively looking for cost savings in areas of product design and through internal and supplier process improvement initiatives? Are you a Lean, Six Sigma practitioner with influence to empower change for continuous improvement.View Details
The first level Team Leader position will have full program and supervisory responsibilities for a small program, subset of a larger program, or functional group conducted under the general supervision of a Manager or Team Leader II. Hold financial accountability for the program or group function and maintain internal or external customer satisfaction by ensuring the manufacture, maintenance or support of quality products, equipment or services delivered within budget and on or ahead of schedule.View Details
As the Principal C++ Software Engineer ... you will design, implement, and deliver reliable, high quality, robust embedded and desktop software targeted to complex medical device instruments meeting regulatory standards. Responsible for daily software activities including participation in issue resolution and communication across discipline teams in order to deliver software projects on-time and on-budget. The Principal C++ Software Engineer position requires a BSCS, BSEE, BS Math, or equivalent discipline (MBA or MS preferred) plus 8 or more years of Medical Device product development experience.View Details
In this position, you will drive design documentation and plans (detailed software design documents, software development plans and software configuration plans). Participate in software project risk assessment including estimates of impact on time, budget, and scope in order to design, implement, and deliver reliable, high quality, robust embedded and desktop software targeted to complex medical instruments meeting regulatory standards.View Details
Do you have 10 or more years of relevant product development experience with demonstrated experience in software development lifecycle (Agile, Spiral), object oriented design methodology and programming languages including one of the following: C#, C++ ? In this role, you will design, implement, and deliver reliable, high quality, robust embedded and desktop software targeted to complex medical instruments meeting regulatory standards.View Details
Perform highly diversified quality assurance functions to evaluate, inspect, test and release assigned company or vendor products, either in-house or at supplier facilities as required. Ensure highest possible product quality and adherence to customer and established requirements and regulations. Perform special evaluative inspections of developmental or manufacturing parts, assemblies, and documentation.View Details
Can you provide technical leadership over complex, major design, development and research projects, develop design and product performance specification requirements and evaluate and select optimum design alternatives as a senior mechanical engineer?View Details
In this role you will have full responsibility for the management and overall success of instrument development programs for the medical device market. This encompasses direction of a disciplined engineering team, monitoring and reporting all aspects of program performance with authority to make decisions to assure the success of the project from inception to completion.View Details
In this role, you will analyze proposed changes to product designs to determine the effect on overall product and system, while ensuring compliance with configuration management policies. Can you oversee and coordinate data management activities for assigned programs in accordance with customer specific requirements and company procedures?View Details
How would you like to lead the design and development of embedded and desktop Graphical User Interfaces (GUIs) for medical device instrumentation? Participate in full product lifecycle development including planning, requirements, design, usability reviews, code, test, release and maintenance.View Details
Would you like to be the software architect who brings our team to the next level? In this role you will architect and design quality embedded and GUI software for integrated complex medical instruments, to be implemented under an FDA compliant product development process. Can you create product proposals with cost and time estimates, while also designing and developing software, architecture components and services to facilitate development and test of production software?View Details
The software engineer will assist in the design, development, testing, and analysis of high quality embedded and desktop software targeted to complex medical instruments meeting regulatory standards. Participate in the development of software design and code, while utilizing software engineering best practices.View Details
Can you perform highly diversified quality assurance functions to evaluate, inspect, test and release assigned company or vendor products? Perform special evaluative inspections of developmental or manufacturing parts, assemblies, and documentation, while ensuring the highest possible product quality and adherence to customer and established requirements and regulations.View Details